Organic dye-photocatalyzed fluoroalkylation of heteroarene-N-oxide derivatives

被引:20
作者
Lantano, Beatriz [1 ]
Barata-Vallejo, Sebastian [1 ]
Postigo, Al [1 ]
机构
[1] Univ Buenos Aires, Fac Farm & Bioquim, Dept Quim Organ, Junin 954, RA-1113 Buenos Aires, DF, Argentina
关键词
ESCHERICHIA-COLI; MILD CONDITIONS; RADICAL-ANION; PERFLUOROALKYLATION; PYRIDINE; ALKYLATION; HYDRAZONES; SALTS; DIFLUOROALKYLATION; SUBSTITUTION;
D O I
10.1039/c8ob01653d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The first direct C-Het-H perfluoroalkylation reaction of heteroaromatic-N-oxides has been achieved through a visible light-photocatalyzed reaction in the presence of commercially available perfluoroalkyl iodides R-F-I and base in DMF as solvent and Rose Bengal as organic photocatalyst. The reactions proceed in the absence of transition metals and can be scaled up. Through an acid-catalyzed transformation of the perfluoroalkylated-N-oxides thus obtained, the first direct syntheses of 2-(perfluoroalkyl)benzo[f][1,3]oxazepines are achieved. De-oxygenation of the resulting perfluoroalkylated heteroaromatic-N-oxides leads to high yielding and regioselective radical perfluoroalkylation protocols of heteroaromatic compounds. To the best of our knowledge, this is the first report on a direct method for perfluoroalkylation of pyridine-, quinoline-, and diazine-N-oxide derivatives.
引用
收藏
页码:6718 / 6727
页数:10
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